Canonical Allele Identifier: CA415196134

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581497C>T (hg19) ; chrX:g.154353129C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353129C>T , CM000685.2:g.154353129C>T	GRCh38
NC_000023.10:g.153581497C>T , CM000685.1:g.153581497C>T	GRCh37
NC_000023.9:g.153234691C>T	NCBI36
NG_011506.1:g.26510G>A
NG_011506.2:g.26510G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6074G>A	ENSP00000353467.4:p.Ser2025Asn
ENST00000369850.10:c.6098G>A MANE Select	ENSP00000358866.3:p.Ser2033Asn
ENST00000369856.8:c.6017G>A	ENSP00000358872.4:p.Ser2006Asn
ENST00000422373.6:c.3161-454G>A	ENSP00000416926.2:n.3161-454G>A
ENST00000610817.5:c.6155G>A	ENSP00000480593.2:n.6155G>A
ENST00000673639.2:c.280-4439G>A
ENST00000676696.1:c.6377G>A	ENSP00000503392.1:n.6377G>A
ENST00000678304.1:n.1277G>A
ENST00000344736.8:c.5978G>A	ENSP00000358863.3:p.Ser1993Asn
ENST00000360319.8:c.6074G>A	ENSP00000353467.4:p.Ser2025Asn
ENST00000369850.7:c.6098G>A	ENSP00000358866.3:p.Ser2033Asn
ENST00000369856.7:c.6017G>A	ENSP00000358872.4:p.Ser2006Asn
ENST00000415241.1:c.300G>A
ENST00000420627.5:c.6054G>A	ENSP00000408921.1:n.6054G>A
ENST00000422373.5:c.6074G>A	ENSP00000416926.1:p.Ser2025Asn
ENST00000444578.1:c.41G>A	ENSP00000397824.1:p.Ser14Asn
ENST00000466325.1:n.237G>A
ENST00000490936.5:n.2087G>A
ENST00000610817.4:c.5844+264G>A	ENSP00000480593.1:n.5844+264G>A
NM_001110556.1:c.6098G>A	NP_001104026.1:p.Ser2033Asn
NM_001456.3:c.6074G>A	NP_001447.2:p.Ser2025Asn
XM_011531127.1:c.6002G>A	XP_011529429.1:p.Ser2001Asn
XM_011531128.1:c.5978G>A	XP_011529430.1:p.Ser1993Asn
XM_011531129.1:c.5924G>A	XP_011529431.1:p.Ser1975Asn
XM_011531130.1:c.5900G>A	XP_011529432.1:p.Ser1967Asn
XM_011531131.1:c.5897G>A	XP_011529433.1:p.Ser1966Asn
NM_001110556.2:c.6098G>A MANE Select	NP_001104026.1:p.Ser2033Asn
NM_001456.4:c.6074G>A	NP_001447.2:p.Ser2025Asn